Canonical Allele Identifier: PA2826162858
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 327980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Thr462Ala
CA9201134
NM_001190716.1:c.1384A>G